CClinicalTrials.gg
CompletedNCT06642103Updated Apr 29, 2025

Pain, Muscle Strength, Motor Imagery, Body Awareness on Function and Individuals With Chronic Lateral Epicondylitis

An observational study in Lateral Epicondylitis, sponsored by KTO Karatay University. Completed at 1 site in Turkey. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2025-04-29.

Sponsored by KTO Karatay University · Observational

Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
108
Ages
18 Years to 65 Years
Sex
All
01

Study summary

The aim of this study was to examine the effect of muscle strength, pain, motor imagery and body awareness on function in individuals with lateral epicondylitis. The main question it aims to answer is: Do pain, motor imagery, muscle strength and body awareness have an impact on function in individuals with lateral epicondylitis?

02

Conditions studied

  • Lateral Epicondylitis
03

In context

Tennis Elbow

284 studies on the registry are indexed under Tennis Elbow; 60 are open to participants now.

This study's enrollment of 108 is above the median of 75 across 26 observational studies indexed under Tennis Elbow.

Browse Tennis Elbow studies →

Lead sponsor

KTO Karatay University is the lead sponsor of 126 studies on the registry; 16 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Lateral epicondylitis

Inclusion criteria

  • a diagnosis of chronic LET by a physician and
  • a pain score > 3 on a visual analog scale (VAS).

Exclusion criteria

Exclusion Criteria:

  • concomitant disorders of the wrist and forearm, such as elbow fracture or dislocation, and treatment with corticosteroid injections within the previous 6 months
05

Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
108 participants (actual)
Target follow-up
1 Day
Patient registry
Yes
06

What researchers measure

Primary outcomes

  1. Function

    Fuction will be evaluated with Patient-Rated Tennis Elbow Evaluation. The Patient-Rated Tennis Elbow Evaluation (PRTEE), is a 15-item questionnaire designed to measure forearm pain and disability in patients with lateral epicondylitis. The PRTEE allows patients to rate their levels of tennis elbow pain and disability from 0 to 10, and consists of 2 subscales: Pain subscale - 5 items (0 = no pain, 10 = worst imaginable) Function subscale (0 = no difficulty, 10 = unable to do) Specific activities - 6 items Usual activities - 4 items

    Time frame: baseline

Secondary outcomes

  1. Pain severity

    The rest, activity and night pains of the participants will be evaluated with a 10 cm Visual Analog Scale before the treatment and at the end of the 4-week application. "0" means no pain, "10" means excruciating pain. Results will be recorded in cm.

    Time frame: Baseline

  2. Motor imagery

    Motor imagery will be assessed through a left/right judgment task in which participants will need to recognize whether hand images correspond to their left or right side using the Recognise™ application (Neuro Orthopaedic Institute, Adelaide, Australia). For this test, participants will be seated comfortably in front of a table, with both elbows flexed at 90◦ and both index fingers placed on the bottom of the screen of an electronic tablet. Forty images of hands (20 on each side) in multiple postures, angles and skin colors will be randomly displayed in the center of the screen of the device. Participants will be given standard instructions to decide as quickly and accurately as possible whether each image is of the right or left hand by clicking on the 'left' (with left fingers) or 'right' (with right fingers) buttons shown at the bottom of the screen.

    Time frame: Baseline

  3. Grip strength

    The maximal grip strength of the patients will be measured with a hydraulic hand dynamometer.

    Time frame: Baseline

  4. The Body Awareness

    The Body Awareness Questionnaire will be used to assess body awareness. The questionnaire consists of 18 questions. Participants will be asked to score each statement on a scale ranging from 1 (1: Not true at all) to 7 (7: Completely true) and the total score will be obtained by summing the score given for each statement.

    Time frame: Baseline

07

Study locations

1 site
  • KTO Karatay University
    Konya, Karatay, Turkey
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 29, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06642103
Lead sponsor
KTO Karatay University
Responsible party
Hasan Gerçek (Principle Investigator, KTO Karatay University) — Principal investigator
First posted
Oct 15, 2024
Start date
Oct 15, 2024
Primary completion
Apr 28, 2025
Completion
Apr 28, 2025
Last update
Apr 29, 2025

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2025. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion